- Confirmed: 这个参考离子已经通过手动审计得到确认和验证。
- Reliable: 这个参考离子可能在特定的解剖组织环境中高度保守。
- Unreliable: 这个参考离子具有较高的排名价值,但缺乏可重复性。
- Unavailable: 由于排名价值低且缺乏可重复性,这个参考离子不应用于注释。
Found 12 Reference Ions Near m/z 274.0429
NovoCell ID | m/z | Mass Window | Metabolite | Ranking | Anatomy Context |
---|---|---|---|---|---|
MSI_000054435 Reliable | 274.0428 | 274.0425 ~ 274.043 MzDiff: 2.0 ppm |
1,3,6-Trihydroxy-5-methoxyxanthone (BioDeep_00000017505) Formula: C14H10O6 (274.0477) |
2.45 (100%) | MALDI - CHCA [NOVOCELL:BACKGROUND] blank |
MSI_000008834 | 274.0437 | 274.0436 ~ 274.0438 MzDiff: 0.6 ppm |
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- (BioDeep_00000172934) Formula: C11H9ClO5 (256.0138) |
1.75 (100%) | Rattus norvegicus [UBERON:0004360] cauda epididymis |
MSI_000016324 Unreliable | 274.0428 | 274.0428 ~ 274.0429 MzDiff: 0.3 ppm |
1,3,6-Trihydroxy-5-methoxyxanthone (BioDeep_00000017505) Formula: C14H10O6 (274.0477) |
1.67 (100%) | Vitis vinifera [PO:0009086] endocarp |
MSI_000003893 Unreliable | 274.0428 | 274.0428 ~ 274.0428 MzDiff: none |
Ferulic acid 4-sulfate (BioDeep_00000025686) Formula: C10H10O7S (274.0147) |
1.39 (100%) | Homo sapiens [UBERON:0002107] liver |
MSI_000012607 Unavailable | 274.043 | 274.043 ~ 274.043 MzDiff: none |
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- (BioDeep_00000172934) Formula: C11H9ClO5 (256.0138) |
-0.07 (100%) | Plant [PO:0005020] vascular bundle |
MSI_000014101 Unavailable | 274.043 | 274.043 ~ 274.043 MzDiff: none |
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- (BioDeep_00000172934) Formula: C11H9ClO5 (256.0138) |
-0.31 (100%) | Plant [PO:0005417] phloem |
MSI_000015316 Unavailable | 274.043 | 274.043 ~ 274.043 MzDiff: none |
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- (BioDeep_00000172934) Formula: C11H9ClO5 (256.0138) |
-0.69 (100%) | Plant [PO:0006036] root epidermis |
MSI_000018553 Unreliable | 274.043 | 274.043 ~ 274.043 MzDiff: none |
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- (BioDeep_00000172934) Formula: C11H9ClO5 (256.0138) |
1.73 (100%) | Plant [PO:0020124] root stele |
MSI_000033547 Unreliable | 274.0428 | 274.0428 ~ 274.0428 MzDiff: none |
1,3,6-Trihydroxy-5-methoxyxanthone (BioDeep_00000017505) Formula: C14H10O6 (274.0477) |
1.73 (100%) | Posidonia oceanica [PO:0005352] xylem |
MSI_000035652 Unavailable | 274.0428 | 274.0428 ~ 274.0428 MzDiff: none |
1,3,6-Trihydroxy-5-methoxyxanthone (BioDeep_00000017505) Formula: C14H10O6 (274.0477) |
-0.23 (100%) | Posidonia oceanica [PO:0006203] pericycle |
MSI_000037147 Unreliable | 274.0425 | 274.0425 ~ 274.0425 MzDiff: none |
1,3,6-Trihydroxy-5-methoxyxanthone (BioDeep_00000017505) Formula: C14H10O6 (274.0477) |
2.04 (100%) | Posidonia oceanica [UBERON:0000329] hair root |
MSI_000040091 Unreliable | 274.043 | 274.043 ~ 274.043 MzDiff: none |
1,3,6-Trihydroxy-5-methoxyxanthone (BioDeep_00000017505) Formula: C14H10O6 (274.0477) |
0.06 (100%) | Posidonia oceanica [PO:0005417] phloem |
Found 24 Sample Hits
Metabolite | Species | Sample | |
---|---|---|---|
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- Formula: C11H9ClO5 (256.0138) Adducts: [M+NH4]+ (Ppm: 17.1) |
Plant (Root) |
MPIMM_035_QE_P_PO_6pmResolution: 30μm, 165x170
|
|
Ferulic acid 4-sulfate Formula: C10H10O7S (274.0147) Adducts: [M-H2O+NH4]+ (Ppm: 17.6) |
Homo sapiens (Liver) |
20171107_FIT4_DHBpos_p70_s50Resolution: 50μm, 70x70
|
|
1,3,6-Trihydroxy-5-methoxyxanthone Formula: C14H10O6 (274.0477) Adducts: [M]+ (Ppm: 15.6) |
Vitis vinifera (Fruit) |
grape_dhb_91_1Resolution: 50μm, 120x114
Grape berries fruit, condition: Ripe |
|
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- Formula: C11H9ClO5 (256.0138) Adducts: [M+NH4]+ (Ppm: 14.9) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito03_17Resolution: 17μm, 208x108
1 male adult wild-type rat was obtained from Inserm U1085 - Irset Research Institute (University of Rennes1, France). Animals were age 60 days and were reared under ad-lib conditions. Care and handling of all animals complied with EU directive 2010/63/EU on the protection of animals used for scientific purposes. The whole epididymis was excised from each animal immediately post-mortem, loosely wrapped rapidly in an aluminum foil and a 2.5% (w/v) carboxymethylcellulose (CMC) solution was poured to embed the epididymis to preserve their morphology. To remove air bubbles, the filled aluminum molds was gently freezed by depositing it on isopentane or dry ice, then on the nitrogen vapors and finally by progressively dipping the CMC/sample coated with aluminum foil into liquid nitrogen (or only flush with liquid nitrogen). Frozen tissues were stored at -80 °C until use to avoid degradation. |
|
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- Formula: C11H9ClO5 (256.0138) Adducts: [M+NH4]+ (Ppm: 14.9) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito03_18Resolution: 17μm, 208x104
|
|
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- Formula: C11H9ClO5 (256.0138) Adducts: [M+NH4]+ (Ppm: 14.1) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_43Resolution: 17μm, 298x106
|
|
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- Formula: C11H9ClO5 (256.0138) Adducts: [M+NH4]+ (Ppm: 14.1) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_44Resolution: 17μm, 299x111
|
|
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- Formula: C11H9ClO5 (256.0138) Adducts: [M+NH4]+ (Ppm: 14.9) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_46Resolution: 17μm, 298x106
|
|
1,3,6-Trihydroxy-5-methoxyxanthone Formula: C14H10O6 (274.0477) Adducts: [M]+ (Ppm: 16) |
Vitis vinifera (Fruit) |
grape_dhb_164_1Resolution: 17μm, 136x122
Grape berries fruit, condition: Late |
|
1,3,6-Trihydroxy-5-methoxyxanthone Formula: C14H10O6 (274.0477) Adducts: [M]+ (Ppm: 15.6) |
Vitis vinifera (Fruit) |
grape_dhb_163_1Resolution: 17μm, 132x115
Grape berries fruit, condition: Late |
|
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- Formula: C11H9ClO5 (256.0138) Adducts: [M+NH4]+ (Ppm: 14.1) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_47Resolution: 17μm, 301x111
|
|
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- Formula: C11H9ClO5 (256.0138) Adducts: [M+NH4]+ (Ppm: 15.2) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito08_48Resolution: 17μm, 294x107
|
|
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- Formula: C11H9ClO5 (256.0138) Adducts: [M+NH4]+ (Ppm: 16) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito01_04Resolution: 17μm, 178x91
|
|
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- Formula: C11H9ClO5 (256.0138) Adducts: [M+NH4]+ (Ppm: 17.1) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito01_03Resolution: 17μm, 159x110
|
|
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- Formula: C11H9ClO5 (256.0138) Adducts: [M+NH4]+ (Ppm: 15.2) |
Rattus norvegicus (normal) |
epik_dhb_head_ito01_05Resolution: 17μm, 183x105
|
|
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- Formula: C11H9ClO5 (256.0138) Adducts: [M+NH4]+ (Ppm: 16.3) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito01_06Resolution: 17μm, 183x103
|
|
1H-2-Benzopyran-7-carboxylic acid, 5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1-oxo- Formula: C11H9ClO5 (256.0138) Adducts: [M+NH4]+ (Ppm: 13.4) |
Rattus norvegicus (Epididymis) |
epik_dhb_head_ito03_14Resolution: 17μm, 205x103
|
|
1,3,6-Trihydroxy-5-methoxyxanthone Formula: C14H10O6 (274.0477) Adducts: [M]+ (Ppm: 16) |
Posidonia oceanica (root) |
20190614_MS1_A19r-20Resolution: 17μm, 262x276
Seagrasses are one of the most efficient natural sinks of carbon dioxide (CO2) on Earth. Despite covering less than 0.1% of coastal regions, they have the capacity to bury up to 10% of marine organic matter and can bury the same amount of carbon 35 times faster than tropical rainforests. On land, the soil’s ability to sequestrate carbon is intimately linked to microbial metabolism. Despite the growing attention to the link between plant production, microbial communities, and the carbon cycle in terrestrial ecosystems, these processes remain enigmatic in the sea. Here, we show that seagrasses excrete organic sugars, namely in the form of sucrose, into their rhizospheres. Surprisingly, the microbial communities living underneath meadows do not fully use this sugar stock in their metabolism. Instead, sucrose piles up in the sediments to mM concentrations underneath multiple types of seagrass meadows. Sediment incubation experiments show that microbial communities living underneath a meadow use sucrose at low metabolic rates. Our metagenomic analyses revealed that the distinct community of microorganisms occurring underneath meadows is limited in their ability to degrade simple sugars, which allows these compounds to persist in the environment over relatively long periods of time. Our findings reveal how seagrasses form blue carbon stocks despite the relatively small area they occupy. Unfortunately, anthropogenic disturbances are threatening the long-term persistence of seagrass meadows. Given that these sediments contain a large stock of sugars that heterotopic bacteria can degrade, it is even more important to protect these ecosystems from degradation. |
|
1,3,6-Trihydroxy-5-methoxyxanthone Formula: C14H10O6 (274.0477) Adducts: [M]+ (Ppm: 16.7) |
Posidonia oceanica (root) |
20190822_MS1_A19r-19Resolution: 17μm, 303x309
Seagrasses are among the most efficient sinks of carbon dioxide on Earth. While carbon sequestration in terrestrial plants is linked to the microorganisms living in their soils, the interactions of seagrasses with their rhizospheres are poorly understood. Here, we show that the seagrass, Posidonia oceanica excretes sugars, mainly sucrose, into its rhizosphere. These sugars accumulate to µM concentrations—nearly 80 times higher than previously observed in marine environments. This finding is unexpected as sugars are readily consumed by microorganisms. Our experiments indicated that under low oxygen conditions, phenolic compounds from P. oceanica inhibited microbial consumption of sucrose. Analyses of the rhizosphere community revealed that many microbes had the genes for degrading sucrose but these were only expressed by a few taxa that also expressed genes for degrading phenolics. Given that we observed high sucrose concentrations underneath three other species of marine plants, we predict that the presence of plant-produced phenolics under low oxygen conditions allows the accumulation of labile molecules across aquatic rhizospheres. |
|
1,3,6-Trihydroxy-5-methoxyxanthone Formula: C14H10O6 (274.0477) Adducts: [M]+ (Ppm: 14.6) |
Posidonia oceanica (root) |
20190613_MS1_A19r-18Resolution: 17μm, 246x264
|
|
1,3,6-Trihydroxy-5-methoxyxanthone Formula: C14H10O6 (274.0477) Adducts: [M]+ (Ppm: 17.1) |
Posidonia oceanica (root) |
20190828_MS1_A19r-22Resolution: 17μm, 292x279
|
|
1,3,6-Trihydroxy-5-methoxyxanthone Formula: C14H10O6 (274.0477) Adducts: [M]+ (Ppm: 15.3) |
Posidonia oceanica (root) |
MS1_20180404_PO_1200Resolution: 17μm, 193x208
|
|
Ferulic acid 4-sulfate Formula: C10H10O7S (274.0147) Adducts: [M-H2O+NH4]+ (Ppm: 9.1) |
Mus musculus (Liver) |
Salmonella_final_pos_recalResolution: 17μm, 691x430
A more complete and holistic view on host–microbe interactions is needed to understand the physiological and cellular barriers that affect the efficacy of drug treatments and allow the discovery and development of new therapeutics. Here, we developed a multimodal imaging approach combining histopathology with mass spectrometry imaging (MSI) and same section imaging mass cytometry (IMC) to study the effects of Salmonella Typhimurium infection in the liver of a mouse model using the S. Typhimurium strains SL3261 and SL1344. This approach enables correlation of tissue morphology and specific cell phenotypes with molecular images of tissue metabolism. IMC revealed a marked increase in immune cell markers and localization in immune aggregates in infected tissues. A correlative computational method (network analysis) was deployed to find metabolic features associated with infection and revealed metabolic clusters of acetyl carnitines, as well as phosphatidylcholine and phosphatidylethanolamine plasmalogen species, which could be associated with pro-inflammatory immune cell types. By developing an IMC marker for the detection of Salmonella LPS, we were further able to identify and characterize those cell types which contained S. Typhimurium.
[dataset] Nicole Strittmatter. Holistic Characterization of a Salmonella Typhimurium Infection Model Using Integrated Molecular Imaging, metabolights_dataset, V1; 2022. https://www.ebi.ac.uk/metabolights/MTBLS2671. |
|
Ferulic acid 4-sulfate Formula: C10H10O7S (274.0147) Adducts: [M-H2O+NH4]+ (Ppm: 19) |
Drosophila melanogaster (brain) |
Drosophila18Resolution: 5μm, 686x685
Sample information
Organism: Drosophila melanogaster
Organism part: Brain
Condition: Healthy
Sample preparation
Sample stabilisation: Frozen
Tissue modification: Frozen
MALDI matrix: 2,5-dihydroxybenzoic acid (DHB)
MALDI matrix application: TM sprayer
Solvent: Aceton/water
MS analysis
Polarity: Positive
Ionisation source: Prototype
Analyzer: Orbitrap
Pixel size: 5μm × 5μm
Annotation settings
m/z tolerance (ppm): 3
Analysis version: Original MSM
Pixel count: 469910
Imzml file size: 696.23 MB
Ibd file size: 814.11 MB |
|